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Differential Diagnosis of metabolic Alkalosis and the overall approach to metabolic alkalosis with cases and step-up scenarios including Saline-Responsive and Unresponsive Types based on Urine Chloride;
Brief yet high-yield review of compensation and how to make sense of compensation formulas in acid-base disorders.
Also discussed: Syndrome of apparent mineralocorticoid excess (SAME, Including Liddle Syndrome), Gitelman & Bartter;
Question-based discussion of the proper framework approach metabolic acidosis, serum versus urinary anion gap, categories of high-anion-gap versus normal anion-gap acidosis and are discussed.
Question-based Discussion of risk factors, workup and management of rhabdomyolysis.
Question-based Review on Differential Diagnosis of Hypercalcemia (Pseudohypercalcemia, PTH-dependent vs PTH-independent Hypercalcemia) and Hypocalcemia; Vitamin D abnormalities, Abnormalities of Phosphate. Also discussed: Workup & Management of Humoral Hypercalcemia of Malignancy, Familial Hypocalciuric Hypercalcemia, Pseudohypoparathyroidism, True Hypoparathyroidism, Primary, 2ndary and tertiary hyperparathyroidism, Medications Side-Effects causing abnormalities of Ca & P.
Question-based Approach to differential diagnosis and hierarchical management in hyperkalemia.
Differential Diagnosis of pseudohypernatremia, Hypovolemic, Euvolemic and Hypervolemic Hypernatremia as well as Differential Diagnosis of pseudohyponatremia vs true hyponatremia is discussed.
A High-yield fully question-based review of childhood vasculitides
The important question is when to suspect vasculitis based on clinical presentation? We discuss differentials and workup (with emphasis on ANCA positivity or negativity or markers of Glomerular involvement) as well as management options and complications (including Mono-neuritis multiplex) for most common classes of vasculitides including Medium-size & Small - vessel Vasculitides including Polyarteritis Nodosa (including updated 3/10 Diagnostic criteria of American College of Rheumatology), Buerger's Disease (Thromboangiitis Oblisterans) Wegener's Granulomatosis, Microscopic Polyangiitis, Churg-Strauss.
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